Impulse oscillometry identifies peripheral airway dysfunction in children with adenosine deaminase deficiency.
Saved in:
| Title: | Impulse oscillometry identifies peripheral airway dysfunction in children with adenosine deaminase deficiency. |
|---|---|
| Authors: | Komarow HD; Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, NIH/NIAID/LAD/Bldg. 10, Room 1C129A1, 10 Center Drive, Bethesda, MD, 20892-1960, USA. komarowh@niaid.nih.gov., Sokolic R; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, 20892, USA. Robert.Sokolic@fda.hhs.gov., Hershfield MS; Department of Biochemistry, Duke University School of Medicine, Durham, NC, USA. michael.hershfield@dm.duke.edu., Kohn DB; Department of Microbiology, Immunology and Molecular Genetics, University of California Los Angeles, David Geffen School of Medicine, Los Angeles, CA, USA. dkohn@mednet.ucla.edu., Young M; Clinical Research Directorate/Clinical Monitoring Research Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Clinical Research, Frederick, MD, 21702, USA. youngmic@mail.nih.gov., Metcalfe DD; Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, NIH/NIAID/LAD/Bldg. 10, Room 1C129A1, 10 Center Drive, Bethesda, MD, 20892-1960, USA. DMETCALFE@niaid.nih.gov., Candotti F; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, 20892, USA. fabio.candotti@chuv.ch.; Division of Immunology and Allergy, University Hospital of Lausanne, CH-1101, Lausanne, Switzerland. fabio.candotti@chuv.ch. |
| Source: | Orphanet journal of rare diseases [Orphanet J Rare Dis] 2015 Dec 18; Vol. 10, pp. 159. Date of Electronic Publication: 2015 Dec 18. |
| Publication Type: | Letter; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
|---|---|
| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 26682746 AccessLevel: 2 PubType: Report PubTypeId: report PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Impulse oscillometry identifies peripheral airway dysfunction in children with adenosine deaminase deficiency. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Komarow+HD%22">Komarow HD</searchLink>; Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, NIH/NIAID/LAD/Bldg. 10, Room 1C129A1, 10 Center Drive, Bethesda, MD, 20892-1960, USA. komarowh@niaid.nih.gov.<br /><searchLink fieldCode="AU" term="%22Sokolic+R%22">Sokolic R</searchLink>; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, 20892, USA. Robert.Sokolic@fda.hhs.gov.<br /><searchLink fieldCode="AU" term="%22Hershfield+MS%22">Hershfield MS</searchLink>; Department of Biochemistry, Duke University School of Medicine, Durham, NC, USA. michael.hershfield@dm.duke.edu.<br /><searchLink fieldCode="AU" term="%22Kohn+DB%22">Kohn DB</searchLink>; Department of Microbiology, Immunology and Molecular Genetics, University of California Los Angeles, David Geffen School of Medicine, Los Angeles, CA, USA. dkohn@mednet.ucla.edu.<br /><searchLink fieldCode="AU" term="%22Young+M%22">Young M</searchLink>; Clinical Research Directorate/Clinical Monitoring Research Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Clinical Research, Frederick, MD, 21702, USA. youngmic@mail.nih.gov.<br /><searchLink fieldCode="AU" term="%22Metcalfe+DD%22">Metcalfe DD</searchLink>; Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, NIH/NIAID/LAD/Bldg. 10, Room 1C129A1, 10 Center Drive, Bethesda, MD, 20892-1960, USA. DMETCALFE@niaid.nih.gov.<br /><searchLink fieldCode="AU" term="%22Candotti+F%22">Candotti F</searchLink>; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, 20892, USA. fabio.candotti@chuv.ch.; Division of Immunology and Allergy, University Hospital of Lausanne, CH-1101, Lausanne, Switzerland. fabio.candotti@chuv.ch. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2015 Dec 18; Vol. 10, pp. 159. <i>Date of Electronic Publication: </i>2015 Dec 18. – Name: TypePub Label: Publication Type Group: TypPub Data: Letter; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101266602 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1750-1172 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217501172%22">17501172 </searchLink><i>NLM ISO Abbreviation: </i>Orphanet J Rare Dis <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=26682746 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-015-0365-z Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 159 Titles: – TitleFull: Impulse oscillometry identifies peripheral airway dysfunction in children with adenosine deaminase deficiency. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Komarow HD – PersonEntity: Name: NameFull: Sokolic R – PersonEntity: Name: NameFull: Hershfield MS – PersonEntity: Name: NameFull: Kohn DB – PersonEntity: Name: NameFull: Young M – PersonEntity: Name: NameFull: Metcalfe DD – PersonEntity: Name: NameFull: Candotti F IsPartOfRelationships: – BibEntity: Dates: – D: 18 M: 12 Text: 2015 Dec 18 Type: published Y: 2015 Identifiers: – Type: issn-electronic Value: 1750-1172 Numbering: – Type: volume Value: 10 Titles: – TitleFull: Orphanet journal of rare diseases Type: main |
| ResultId | 1 |